Binder for Secondary Battery, Negative Electrode for Secondary Battery Including the Same, and Lithium Secondary Battery Including the Same

ABSTRACT

Provided are a binder for a secondary battery, a negative electrode including the same, and a secondary battery including the same. More particularly, the binder for a secondary battery including a crosslinked product of a copolymer with a silane-based crosslinking agent according to the present invention may have excellent thermal resistance and mechanical properties and effectively improve a binding force, and the negative electrode for a secondary battery and the secondary battery including the same may effectively suppress expansion of a negative electrode to improve charge/discharge cycle characteristics and performance of the secondary battery.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to Korean Patent Application No. 10-2021-0141359, filed Oct. 21, 2021, the disclosure of which is hereby incorporated by reference in its entirety.

BACKGROUND OF THE INVENTION Field of the Invention

The following disclosure relates to a binder for a secondary battery, a negative electrode including the same, and a secondary battery including the same.

More particularly, the following disclosure relates to a negative electrode for a secondary battery having excellent thermal resistance and mechanical properties and an improved binding force, by using a crosslinked product of the copolymer with the silane-based crosslinking agent according to the present invention as a binder, and a secondary battery including the same.

In addition, a secondary battery manufactured with a negative electrode including the binder may suppress expansion of a negative electrode to significantly improve charge/discharge cycle characteristics and performance of the secondary battery.

Description of Related Art

As a secondary battery application range is expanded to electric vehicles and power storage, a demand for developing an electrode having high stability, long life, high energy density, and high output properties is growing.

A lithium secondary battery may be a battery including a positive electrode including a positive electrode active material capable of inserting/desorbing lithium ions, a negative electrode including a negative electrode active material, a microporous separator between the positive electrode and the negative electrode, and a nonaqueous electrolyte.

Among them, as a negative electrode active material, a silicon-based active material is increasingly used due to a significantly increased charge and discharge capacity, but the volume expands by a lithium ion during charging and discharging, thereby greatly affecting the stability of the battery. For example, when a silicon-based material is used as the negative electrode active material, the volume may be increased up to 300% in some cases, and thus, there is a limitation to using it, which causes charge and discharge characteristics to be significantly lowered.

In order to solve the problem, a technology of a binder for a negative electrode active material has been developed. For example, in order to suppress a change in volume due to the charge and discharge of, in particular, a silicon-based negative electrode active material as described above, a technology of forming a negative electrode active material layer using a binder such as carboxymethyl cellulose (CMC) and styrene butadiene rubber (SBR) as a binder of a negative electrode active material has been developed. However, the binder for a negative electrode active material may partly solve the problem of excessive volume expansion, but there is still a need to suppress volume expansion, and also, there is still a problem in that due to its low adhesion, an active material is desorbed as charge and discharge progress, thereby deteriorating battery characteristics.

Therefore, there is a need to develop a novel binder for a negative electrode active material, which suppresses a change in volume of an electrode occurring as charge and discharge progress, retains sufficient adhesive strength to prevent deterioration of battery performance due to release or desorption of an active material, and is not deteriorated.

In addition, a novel binder for a secondary battery, which may promote battery life and performance improvement by developing a binder having the characteristics, is demanded.

SUMMARY OF THE INVENTION

An embodiment of the present invention is directed to providing a binder for a secondary battery which suppresses the expansion of a negative electrode and improves the charge/discharge cycle characteristics and the performance of a secondary battery, a negative electrode including the same, and a secondary battery including the same.

Another embodiment of the present invention is directed to providing a binder for a secondary battery which has excellent thermal resistance and mechanical properties and an improved binding force, a negative electrode including the same, and a secondary battery including the same.

Still another embodiment of the present invention is directed to providing a negative electrode slurry composition for a secondary battery which improves the coatability and the adhesion of a binder for a secondary battery to suppress the exfoliation and desorption of a negative electrode active material, thereby having improved battery performance. In one general aspect, a binder for a secondary battery the binder includes a copolymer which is crosslinked with a silane-based crosslinking agent, wherein the copolymer comprises a repeating unit (a) of the following Chemical Formula 1, a repeating unit (b) of the following Chemical Formula 2, a repeating unit (c) of the following Chemical Formula 3, and a repeating unit (d) of the following Chemical Formula 4:

wherein

R₁ and R₃ are independently substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms;

R₂ and R₄ are independently hydrogen or substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms;

M^(n+) is a cation having an oxidation number of n except for a hydrogen ion; and

n is an integer of 1 to 3.

In the copolymer according to an exemplary embodiment, (a+b):(c+d) may be 0.05 to 0.95:0.95 to 0.05, wherein a, b, c, and d are mole fractions of the repeating units (a), (b), (c), and (d), respectively in the copolymer.

In the binder for a secondary battery according to an exemplary embodiment, the copolymer may satisfy the following Equation 1:

0.45<(b+d)/(a+b+c+d)<1.0   [Equation 1]

wherein a, b, c, and d are mole fractions of the repeating units (a), (b), (c), and (d), respectively in the copolymer.

In the binder for a secondary battery according to an exemplary embodiment, the silane-based crosslinking agent may be represented by the following Chemical Formula 5:

(R₅O)_(x)Si(R₆)_(y)   [Chemical Formula 5]

wherein x+y=4, and x is 2 or 3;

R₅ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms;

R₆ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms or heterohydrocarbyl having 1 to 7 carbon atoms;

the hydrocarbyl and the heterohydrocarbyl may be optionally substituted by one or more selected from glycidyl, amino, and cyano; and

when y is 2, each R₆ may be the same as or different from each other.

In the binder for a secondary battery according to an exemplary embodiment, an example of the silane-based crosslinking agent may be one or two or more selected from the group consisting of dimethyldimethoxysilane, diethoxydimethylsilane, methyltriethoxysilane, (3-glycidoxypropyl)methyldimethoxysilane, (3-glycidoxypropyl)methyldiethoxysilane, (3-glycidoxypropyl)trimethoxysilane, (3-glycidoxypropyl)triethoxysilane, (3-aminopropyl)methyldimethoxysilane, (3-aminopropyl)methyldiethoxysilane, (3-aminopropyl)trimethoxysilane, (3-aminopropyl)triethoxysilane, [3-(2-aminoethylamino)propyl]methyldimethoxysilane, [3-(2-aminoethylamino)propyl]methyldiethoxysilane, [3-(2-aminoethylamino)propyl]triethoxysilane, [3-(2-aminoethylamino)propyl]trimethoxysilane, 3-(trimethoxysilyl)propionitrile, 3-(triethoxysilyl)propionitrile, and the like, but is not limited thereto as long as Chemical Formula 5 is satisfied.

In the binder for a secondary battery according to an exemplary embodiment, the silane-based crosslinking agent may be one or a combination of two or more selected from the group consisting of (3-aminopropyl)triethoxysilane, [3-(2-aminoethylamino)propyl]trimethoxysilane, and the like, but is not limited thereto as long as Chemical Formula 5 is satisfied.

In the binder for a secondary battery according to an exemplary embodiment, the content of the silane-based crosslinking agent is not limited as long as the purpose of the present invention is achieved, but, for example, may be 0.1 to 20 wt % with respect to the binder for a secondary battery.

In the binder for a secondary battery according to an exemplary embodiment, the binder for a secondary battery may be a binder for a lithium secondary battery negative electrode.

In another general aspect, a secondary battery includes a positive electrode and a negative electrode for a secondary battery wherein the negative electrode for a secondary battery includes a current collector; and a negative electrode active material layer disposed on the current collector, and the negative electrode active material layer includes the binder for a secondary battery described above and a negative electrode active material.

In the secondary battery according to an exemplary embodiment, the negative electrode active material may include a silicon-based active material.

In the secondary battery according to an exemplary embodiment, the negative electrode active material may further include a graphite-based active material.

In the secondary battery according to an exemplary embodiment, a mass ratio between the silicon-based active material and the graphite-based active material may be 97:3 to 3:97.

In the secondary battery according to an exemplary embodiment, the binder for a secondary battery may be included at 0.1 to 30 wt % with respect to the negative electrode active material layer.

In still another general aspect, a method of preparing a binder for a secondary battery includes: (A) saponifying a copolymer including a repeating unit (a) of the following Chemical Formula 1 and a repeating unit (c) of the following Chemical Formula 3 to prepare a saponified copolymer; and

(B) reacting the saponified copolymer with a silane-based crosslinking agent to perform crosslinking,

wherein the saponified copolymer includes the repeating unit (a) of the following Chemical Formula 1, a repeating unit (b) of the following Chemical Formula 2, the repeating unit (c) of the following Chemical Formula 3, and a repeating unit (d) of the following Chemical Formula 4:

wherein

R₁ and R₃ are independently substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms;

R₂ and R₄ are independently hydrogen or substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms;

M^(n+) is a cation having an oxidation number of n except for a hydrogen ion; and

n is an integer of 1 to 3.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, a degree of saponification in step (A) may be more than 0.45 and less than 1.0, and the degree of saponification may be calculated by (b+d)/(a+b+c+d), wherein a, b, c, and d are mole fractions of the repeating units (a), (b), (c), and (d) in the saponified copolymer.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the silane-based crosslinking agent may be represented by the following Chemical Formula 5:

(R₅O)_(x)Si(R₆)_(y)   [Chemical Formula 5]

wherein x+y=4, and x is 2 or 3;

R₅ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms;

R₆ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms or heterohydrocarbyl having 1 to 7 carbon atoms;

the hydrocarbyl and the heterohydrocarbyl may be optionally substituted by one or more selected from glycidyl, amino, and cyano; and

when y is 2, each R₆ may be the same as or different from each other.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the silane-based crosslinking agent may be, for example, one or two or more selected from the group consisting of dimethyldimethoxysilane, diethoxydimethylsilane, methyltriethoxysilane, (3-glycidoxypropyl)methyldimethoxysilane, (3-glycidoxypropyl)methyldiethoxysilane, (3-glycidoxypropyl)trimethoxysilane, (3-glycidoxypropyl)triethoxysilane, (3-aminopropyl)methyldimethoxysilane, (3-aminopropyl)methyldiethoxysilane, (3-aminopropyl)trimethoxysilane, (3-aminopropyl)triethoxysilane, [3-(2-aminoethylamino)propyl]methyldimethoxysilane, [3-(2-aminoethylamino)propyl]methyldiethoxysilane, [3-(2-aminoethylamino)propyl]triethoxysilane, [3-(2-aminoethylamino)propyl]trimethoxysilane, 3-(trimethoxysilyl)propionitrile, 3-(triethoxysilyl)propionitrile, and the like, but is not limited thereto as long as Chemical Formula 5 is satisfied.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the silane-based crosslinking agent may be one or a combination of two or more selected from the group consisting of (3-aminopropyl)triethoxysilane, [3-(2-aminoethylamino)propyl]trimethoxysilane, and the like, but is not limited thereto as long as Chemical Formula 5 is satisfied.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the content of the silane-based crosslinking agent is not particularly limited, but, for example, may be 0.1 to 20 wt % with respect to the binder for a secondary battery.

Other features and aspects will be apparent from the following detailed description, the drawings, and the claims.

DESCRIPTION OF THE INVENTION

Hereinafter, the present disclosure will be described in more detail. However, the following examples or exemplary embodiments are only a reference for describing the present disclosure in detail, and the present disclosure is not limited thereto and may be implemented in various forms.

In addition, unless otherwise defined, all technical terms and scientific terms have the same meanings as those commonly understood by one of those skilled in the art to which the present disclosure pertains.

The terms used herein are only for effectively describing a certain exemplary example, and are not intended to limit the present invention.

In addition, the singular form used in the specification and claims appended thereto may be intended to include a plural form also, unless otherwise indicated in the context.

In addition, units used in the present specification without particular mention are based on weights, and as an example, a unit of % or ratio refers to a wt % or a weight ratio and wt % refers to wt % of any one component in a total composition, unless otherwise defined.

In addition, unless particularly described to the contrary, “comprising” or “including” any elements will be understood to imply further inclusion of other elements rather than the exclusion of any other elements.

In addition, the numerical range used in the present specification may include all values within the range including the lower limit and the upper limit, increments logically derived in a form and span in a defined range, all double limited values, and all possible combinations of the upper limit and the lower limit in the numerical range defined in different forms. Unless otherwise particularly defined in the present specification, values which may be outside a numerical range due to experimental error or rounding off are also included in the defined numerical range.

A “hydrocarbon” described in the present specification refers to a chemical group containing only hydrogen and carbon atoms.

“Hydrocarbyl” or “heterohydrocarbyl” described in the present specification refers to a radical having one bonding site derived from a hydrocarbon or heterohydrocarbon, and “hetero-” means that carbon is substituted by one or more heteroatoms selected from B, O, N, C(═O), P, P(═O), S, S(═O)₂, and a Si atom.

Hereinafter, the present disclosure will be described in more detail.

The present disclosure relates to a binder for a secondary battery including a crosslinked product prepared by reacting a copolymer for a binder for a secondary battery having specific repeating units and a silane-based crosslinking agent which is crosslinkable with the copolymer. A negative electrode manufactured by mixing the binder with a negative electrode active material and a secondary battery including the negative electrode have excellent thermal resistance and mechanical properties and an improved binding force, thereby effectively suppressing expansion even when a silicon-based negative electrode active material is used, and thus, a negative electrode for a secondary battery having excellent battery performance and a secondary battery including the same may be provided.

The binder for a secondary battery has excellent mechanical properties and binding force to suppress exfoliation and desorption of the negative electrode active material, and when a negative electrode is manufactured by including the binder, a negative electrode for a secondary battery having improved battery performance may be manufactured.

In addition, since a negative electrode including the binder for a secondary battery according to an exemplary embodiment may effectively suppress expansion, a negative electrode having improved charge/discharge cycle characteristics and performance of a secondary battery and a secondary battery including the same may be provided.

The binder for a secondary battery according to an exemplary embodiment includes a copolymer which is crosslinked with a silane-based crosslinking agent, wherein the copolymer comprises a repeating unit (a) of the following Chemical Formula 1, a repeating unit (b) of the following Chemical Formula 2, a repeating unit (c) of the following Chemical Formula 3, and a repeating unit (d) of the following Chemical Formula 4:

The binder for a secondary battery according to an exemplary embodiment may be prepared by a crosslinking reaction between a copolymer including a repeating unit (a) of the following Chemical Formula 1, a repeating unit (b) of the following Chemical Formula 2, a repeating unit (c) of the following Chemical Formula 3, and a repeating unit (d) of the following Chemical Formula 4 and a silane-based crosslinking agent. In addition, the binder may include a crosslinked product prepared by the crosslinking reaction and, the crosslinked product may refer to a crosslinked product of the copolymer with the silane-based crosslinking agent. Here, the crosslinking reaction may refer to crosslinking in one copolymer chain or between two or more copolymer chains different from each other.

wherein R₁ and R₃ are independently substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms; R₂ and R₄ are independently hydrogen or substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms; M^(n+) is a cation having an oxidation number of n except for a hydrogen ion; and n is an integer of 1 to 3.

Specifically, an example of R₁ and R₃ may be independently alkyl having 1 to 5 carbon atoms, and a specific example thereof may be methyl, ethyl, or propyl. An example of R₂ and R₄ may be independently hydrogen or alkyl having 1 to 5 carbon atoms, and specifically, may be hydrogen or methyl.

An exemplary embodiment of the repeating unit (a) of Chemical Formula 1 may be a vinyl acetate-derived unit, an exemplary embodiment of the repeating unit (b) of Chemical Formula 2 may be a vinyl alcohol-derived unit, an exemplary embodiment of the repeating unit (c) of Chemical Formula 3 may be a (meth)acrylate-derived unit, and an exemplary embodiment of the repeating unit (d) of Chemical Formula 4 may be an ionized substituted (meth)acrylic acid-derived unit. The (meth)acrylate may include both acrylate or methacrylate, and the (meth)acrylic acid may include both acrylic acid or methacrylic acid.

A cation of a salt of the ionized substituted (meth)acrylic acid(M^(n+)) may be an alkali metal ion when n is 1, specifically, may be at least one selected from a sodium ion, a potassium ion, a lithium ion, and the like, and may be an ammonium ion (NH₄ ⁺). In addition, when n is 2, it may be an alkaline earth metal ion, and specifically, may be a calcium ion or a magnesium ion. When n is 3, it may be an ion of a metal such as Al or Ga, but is not particularly limited as long as it is a metal ion commonly known to a person skilled in the art.

The binder for a secondary battery prepared by including the copolymer including the repeating units (a) to (d) may improve a binding force between a negative electrode current collector and a negative electrode active material layer or of a negative electrode active material layer to suppress the exfoliation and the desorption of a negative electrode active material and improve the strength and the flexibility of the negative electrode active material layer. In addition, even a silicon-based negative electrode active material effectively suppresses expansion to exert an effect of stabilizing battery performance.

In the binder for a secondary battery according to an exemplary embodiment, the binder for a secondary battery may be a binder for a lithium secondary battery negative electrode or a binder for a lithium secondary battery positive electrode, and specifically, may be a binder for a lithium secondary battery negative electrode.

In the binder for a secondary battery according to an exemplary embodiment, the copolymer may be a random copolymer, a block copolymer, or a tapered copolymer in which the repeating units (a) to (d) form a backbone, and the kind is not limited.

Specifically, a random copolymer including the repeating units (a) to (d) may be preferred, since it has excellent solubility in water to improve processability when a negative electrode slurry composition for a secondary battery is manufactured, and has sufficient tensile strength and flexibility to improve the strength and the flexibility of the negative electrode active material layer.

In the binder for a secondary battery according to an exemplary embodiment, the copolymer may further include a repeating unit derived from a commonly used or known monomer, except an aromatic vinyl-based monomer, a conjugated diene-based monomer, and a (meth)acrylonitrile-based monomer. When the copolymer includes an additional repeating unit derived from an aromatic vinyl-based monomer such as styrene, a conjugated diene-based monomer such as 1,3-butadiene, and a (meth)acrylonitrile-based monomer, a low expansion rate and excellent charge/discharge cycle characteristics and battery performance of a secondary battery which are intended in the present disclosure may not be implemented, which is thus not preferred, and, in particular, the copolymer including the repeating unit derived from a styrene monomer interferes with formation of a dense crosslinked structure by the effect of steric hindrance of a side chain, and thus, a high expansion rate and low secondary battery performance may be shown.

In the binder for a secondary battery according to an exemplary embodiment, (a+b):(c+d) of the copolymer may be at a mole fraction ratio of 0.05 to 0.95:0.95 to 0.05, specifically 0.1 to 0.9:0.9 to 0.1, and more specifically, may be at a mole fraction ratio of 0.2 to 0.8:0.8 to 0.2.

In the binder for a secondary battery according to an exemplary embodiment, a and b of the copolymer may be included at a mole fraction ratio of a:b of 0.05 to 0.9:0.95 to 0.1, specifically 0.1 to 0.6:0.9 to 0.4, and more specifically 0.15 to 0.45:0.85 to 0.55.

In the binder for a secondary battery according to an exemplary embodiment, c and d of the copolymer may be included at a mole fraction ratio of c:d of 0.05 to 0.6:0.95 to 0.4, specifically 0.1 to 0.45:0.9 to 0.55, and more specifically 0.15 to 0.4:0.85 to 0.6.

In the binder for a secondary battery according to an exemplary embodiment, the copolymer may satisfy the following Equation 1, and specifically, may satisfy the following Equation 2:

0.45<(b+d)/(a+b+c+d)<1.0   [Equation 1]

0.5<(b+d)/(a+b+c+d)<0.95   [Equation 2]

wherein a, b, c, and d are mole fractions of the repeating units (a), (b), (c), and (d), respectively in the copolymer.

The binder for a secondary battery including the copolymer satisfying Equation 1 or 2 has better tensile strength and adhesion, and also, when a negative electrode slurry composition for a secondary battery is prepared by including the binder, the composition may have no agglomeration and improved coatability, which is thus more preferred, but the present disclosure is not limited thereto. In addition, the copolymer satisfying Equation 1, specifically Equation 2, may further improve the adhesion of the binder for a secondary battery to suppress the exfoliation and desorption of the negative electrode active material from a current collector. When a negative electrode is manufactured using the binder for a secondary battery having improved coatability and adhesion as such, a binding force between the negative electrode active material and the current collector may be improved to effectively suppress the expansion of the negative electrode, and also, the charge/discharge cycle characteristics and the performance of the secondary battery manufactured using the negative electrode are improved, which is thus preferred, but the present disclosure is not limited thereto, as long as the purpose of the present disclosure is achieved.

In the binder for a secondary battery according to an exemplary embodiment, the copolymer may have a weight average molecular weight of 100,000 to 2,000,000 Da. For example, the copolymer may have a weight average molecular weight of 200,000 to 1,800,000 Da. Specifically, the copolymer may have a weight average molecular weight of 400,000 to 1,600,000 Da. More specifically, the copolymer may have a weight average molecular weight of 500,000 to 1,500,000 Da, but is not limited thereto. The binder for a secondary battery manufactured using the copolymer satisfying the range may have more improved adhesion.

The copolymer may be prepared by various known methods such as emulsion polymerization, suspension polymerization, solution polymerization, and bulk polymerization.

In the binder for a secondary battery according to an exemplary embodiment, the silane-based crosslinking agent may be represented by the following Chemical Formula 5:

(R₅O)_(x)Si(R₆)_(y)   [Chemical Formula 5]

wherein x+y=4, and x is 2 or 3; R₅ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms; R₆ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms or heterohydrocarbyl having 1 to 7 carbon atoms; and the hydrocarbyl and the heterohydrocarbyl may be optionally substituted by one or more selected from glycidyl, amino, and cyano; and when y is 2, R₆ may be the same as or different from each other. Here, “Substituted” means that the hydrogen atom of the moiety being substituted (eg, hydrocarbyl or heterohydrocarbyl) is replaced by a substituent (one or more selected from glycidyl, amino, and cyano).

In the binder for a secondary battery according to an exemplary embodiment, Chemical Formula 5 may be represented by the following Chemical Formula 6 or 7:

wherein R₇ to R₉ and R₁₁ to R₁₂ are independently substituted or unsubstituted alkyl having 1 to 7 carbon atoms; R₁₀, R₁₃, and R₁₄ are independently substituted or unsubstituted alkyl having 1 to 7 carbon atoms or heteroalkyl having 1 to 7 carbon atoms; and optionally the alkyl and the heteroalkyl may be independently substituted by one or more selected from glycidyl, amino, and cyano. Specifically, R₁₀, R₁₃, and R₁₄ may be independently —(R₁₅)X, —(R₁₅)O(R₁₆)X, or —(R₁₅)NH(R₁₆)X, R₁₅ and R₁₆ may be independently a direct bond or alkylene having 1 to 7 carbon atoms, and X may be glycidyl, amino, or cyano. Here, “Substituted” means that the hydrogen atom of the moiety being substituted (eg, alkyl or heteroalkyl) is replaced by a substituent (one or more selected from glycidyl, amino, and cyano).

In the binder for a secondary battery according to an exemplary embodiment, the silane-based crosslinking agent may be one or two or more selected from the group consisting of dimethyldimethoxysilane, diethoxydimethylsilane, methyltriethoxysilane, (3-glycidoxypropyl)methyldimethoxysilane, (3-glycidoxypropyl)methyldiethoxysilane, (3-glycidoxypropyl)trimethoxysilane, (3-glycidoxypropyl)triethoxysilane, (3-aminopropyl)methyldimethoxysilane, (3-aminopropyl)methyldiethoxysilane, (3-aminopropyl)trimethoxysilane, (3-aminopropyl)triethoxysilane, [3-(2-aminoethylamino)propyl]methyldimethoxysilane, [3-(2-aminoethylamino)propyl]methyldiethoxysilane, [3-(2-aminoethylamino)propyl]triethoxysilane, [3-(2-aminoethylamino)propyl]trimethoxysilane, 3-(trimethoxysilyl)propionitrile, 3-(triethoxysilyl)propionitrile, and the like, but is not limited thereto.

Specifically, the silane-based crosslinking agent may be one or a combination of two or more selected from the group consisting of (3-aminopropyl)triethoxysilane, [3-(2-aminoethylamino)propyl]trimethoxysilane, and the like, and when the silane-based crosslinking agent is used, a binder for a secondary battery including a crosslinked product having a higher crosslinking degree may be prepared, and thus, a secondary battery showing more improved charge/discharge cycle characteristics and battery performance may be manufactured using the same.

In the binder for a secondary battery according to an exemplary embodiment, the silane-based crosslinking agent may be included at 0.1 to 20 wt %, specifically 1 to 17 wt %, and more specifically 5 to 15 wt % with respect to the total weight of the binder for a secondary battery based on a dry weight, and may be crosslinked with the copolymer, but is not limited thereto. When the content range is satisfied, the expansion of a negative electrode is effectively suppressed, thereby showing a lower expansion rate and an improved capacity retention rate to effectively improve the charge/discharge cycle characteristics and the performance of the secondary battery, which is thus preferred.

In the binder for a secondary battery according to an exemplary embodiment, the copolymer and the silane-based crosslinking agent may satisfy a weight ratio of 80 to 99.9:20 to 0.1, and they may be reacted to prepare a crosslinked product. Specifically, a weight ratio of 83 to 99:17 to 1, more specifically 85 to 95:15 to 5 may be satisfied.

In the binder for a secondary battery according to an exemplary embodiment, a binder for a secondary battery including a crosslinked product obtained by crosslinking a copolymer including a repeating unit (a) of the following Chemical Formula 1, a repeating unit (b) of the following Chemical Formula 2, a repeating unit (c) of the following Chemical Formula 3, and a repeating unit (d) of the following Chemical Formula 4 and the silane-based crosslinking agent; the copolymer; and the silane-based crosslinking agent may be provided. Specifically, a case in which only a part of the added amount in a binder composition including the copolymer and the silane-based crosslinking agent is crosslinked to be a crosslinked product, and the remaining is present in an uncrosslinked state may be included. A binder for a secondary battery including the uncrosslinked copolymer and the crosslinking agent may be crosslinked to produce a crosslinked product in the later step, but the present disclosure is not limited thereto.

A secondary battery manufactured using the binder for a secondary battery according to an exemplary embodiment may effectively suppress the expansion of a negative electrode, thereby showing lower expansion rate and an improved capacity retention rate to effectively improve the charge/discharge cycle characteristics and the performance of the secondary battery.

The present disclosure may provide a negative electrode slurry composition for a secondary battery including the binder for a secondary battery described above and a negative electrode active material.

The negative electrode active material may be one or a combination of two or more selected from the group consisting of graphite-based active materials, platinum, palladium, silicon-based active material, silver, aluminum, bismuth, tin, zinc, silicon-carbon composite materials, and the like. For example, it may be more preferred to use a negative electrode active material including a silicon-based active material since better effects are shown, but it is preferred in terms of suppressing expansion, and it is not limited in terms of excellent binding force or electrical properties. In a preferred exemplary embodiment, the negative electrode active material may include a silicon-based active material and further include a graphite-based active material, and a mass ratio between the silicon-based active material and the graphite-based active material may satisfy 3 to 97:97 to 3 or 10 to 90:90 to 10, but is not limited thereto.

The silicon-based active material may include a silicon-based material, for example, Si, SiO_(x) (0<x<2), Si-Q alloys (Q is one or a combination of two or more selected from the group consisting of alkali metals, alkaline earth metals, Group 13 element, Group 14 elements, Group 15 elements, Group 16 elements, transition metals, rare earth elements, and the like, except Si and C), silicon-carbon composites, and the like. The silicon-carbon composite may include, for example, silicon carbide (SiC) or silicon-carbon particles having a core-shell structure, and as a non-limiting example, may be formed by depositing a silicon layer on a graphite core surface. As another example, the silicon-carbon particles may be formed by coating commercially available graphite particles with a silicon layer by a chemical vapor deposition (CVD) process using a silicon precursor compound such as a silane-based compound. In some exemplary embodiments, the particles may further include amorphous carbon coating, but are not limited thereto.

The graphite-based active material may be artificial graphite or a mixture of artificial graphite and natural graphite. The graphite-based active material may have an average particle diameter (D50) of 5 to 30 μm, specifically 8 to 20 μm, and may be amorphous, plate-like, flaky, spherical, or fibrous, but is not limited thereto. Meanwhile, when the graphite-based active material is a mixture of artificial graphite and natural graphite, specifically, the content of the artificial graphite may be equivalent to or higher than the content of the natural graphite, and the artificial graphite and the natural graphite may be included at a weight ratio of 50 to 95:50 to 5, specifically 50 to 90:50 to 10, and more specifically 60 to 90:40 to 10. Thus, adhesive strength between a current collector and an active material layer may be further improved, and a high-rate charge capacity retention rate and charge/discharge cycle characteristics of a battery may be improved.

The negative electrode slurry composition for a secondary battery according to an exemplary embodiment may further include a conductive material and a solvent.

The conductive material is used for imparting conductivity to an electrode, and may be used without significant limitation as long as it is an electronically conductive material without causing a chemical change in a battery, and as the conductive material, one or a combination of two or more selected from the group consisting of graphite-based conductive materials, carbon black-based conductive materials, graphene, carbon nanotubes, metal and metal compound-based conductive materials, and the like may be used. A non-limiting example of the carbon black-based conductive material may include acetylene black, ketjen black, denka black, thermal black, channel black, and the like; a non-limiting example of the carbon nanotubes may include single-walled carbon nanotubes (SWCNT), double-walled carbon nanotubes (DWCNT), multi-walled carbon nanotubes (MWCNT), rope carbon nanotubes, and the like; and a non-limiting example of metal-based or metal compound-based conductive materials may include tin, tin oxide, tin phosphate (SnPO₄), titanium oxide, potassium titanate, perovskite materials such as LaSrCoO₃ and LaSrMnO₃, and the like, but is not limited to the listed conductive materials. The conductive material may be included at 0.05 to 30 wt % with respect to the total weight of the negative electrode active material layer, but the content of the conductive material may be appropriately adjusted depending on its application purpose and physical properties. The solvent is a solvent for forming a negative electrode slurry composition for a secondary battery, and may be an aqueous solvent such as water. The solvent may be used at a content to allow the composition to have appropriate viscosity, considering the applicability and coatability of the negative electrode slurry composition for a secondary battery. Otherwise, an organic solvent or a mixed solvent of an organic solvent and water may be used as needed. When an organic solvent is used, a non-limiting example thereof may be alcohol, ether, ester, ketone, hydrocarbon, and the like, and is not limited thereto as long as the binder for a secondary battery according to the present invention is dissolved therein.

The solid content of the negative electrode slurry composition for a secondary battery according to an exemplary embodiment may be 1 wt % or more, 5 wt % or more, 10 wt % or more, 20 wt % or more, 35 wt % or more, 40 wt % or more, 45 wt % or more, or 50 wt % or more, and though the upper limit is not limited, may be 60 wt % or less, 70 wt % or less, or 80 wt % or less, or 95 wt % or less, and is not limited thereto.

The present disclosure may provide a negative electrode for a secondary battery including a current collector and a negative electrode active material layer disposed on the current collector, wherein specifically, the negative electrode active material layer includes the binder for a secondary battery described above.

The current collector may be one or a combination of two or more selected from the group consisting of copper foil, nickel foil, stainless foil, titanium foil, nickel foam, copper foam, a polymer substrate coated with a conductive metal, and the like, but is not limited thereto, and materials known in the art may be used without limitation.

In the negative electrode for a secondary battery according to an exemplary embodiment, the binder for a secondary battery may be included at 0.1 to 30 wt % with respect to the total weight of the negative electrode active material layer, based on a dry weight. Specifically, it may be 0.5 to 20 wt %, more specifically 1 to 10 wt o, but the content of the binder is not particularly limited as long as the performance of a secondary battery to be desired in the present disclosure is not impaired. When the content range is satisfied, the expansion of a negative electrode and the desorption of a negative electrode active material occurring during charging and discharging may be effectively suppressed, thereby implementing the further improved capacity and energy density of the secondary battery.

The negative electrode active material layer may be prepared from the negative electrode slurry composition for a secondary battery described above.

The negative electrode active material layer may have a thickness of 1 to 150 μm, specifically 10 to 100 μm, and more specifically 20 to 80 μm, but is not limited thereto. The thickness may be adjusted by coating an appropriate coating amount depending on the solid content of the negative electrode slurry composition for a secondary battery described above, and specifically, the coating amount may be 0.1 to 20 mg/cm², specifically 1 to 10 mg/cm², but is not limited thereto.

The present disclosure may provide a secondary battery including a positive electrode and a negative electrode for a secondary battery, wherein the negative electrode for a secondary battery includes a current collector; and a negative electrode active material layer disposed on the current collector, and the negative electrode active material layer includes the binder for a secondary battery described above and a negative electrode active material. Here, since the binder for a secondary battery, the negative electrode active material, the negative electrode active material layer, the current collector, and the negative electrode for a secondary battery are as described above, the detailed description thereof will be omitted.

Specifically, the secondary battery may include the negative electrode for a secondary battery, a positive electrode, and an electrolyte, and may further include a separator interposed between the positive electrode and the negative electrode.

The positive electrode may include a current collector; and a positive electrode active material layer formed by applying a composition for a positive electrode including a positive electrode active material on the current collector. The current collector may be a negative electrode current collector described above, and any material known in the art may be used, but is not limited thereto. In addition, the positive electrode active material layer may include a positive electrode active material, and optionally, may further include a binder for a positive electrode and a conductive material. The positive electrode active material may be any positive electrode active material known in the art, and may be, for example, a composite oxide of lithium with a metal selected from cobalt, manganese, nickel, and a combination thereof, but is not limited thereto. The binder for a positive electrode and the conductive material may be the binder for a secondary battery and the conductive material described above, and any materials known in the art may be used, but the present disclosure is not limited thereto.

The electrolyte may be an electrolyte solution including an organic solvent and a lithium salt. The organic solvent serves as a medium in which ions involved in the electrochemical reaction of the battery may move, and for example, carbonate-based, ester-based, ether-based, ketone-based, alcohol-based, or aprotic solvents may be used, the organic solvent may be used alone or in combination of two or more, and when used in combination of two or more, a mixing ratio may be appropriately adjusted depending on battery performance to be desired. Meanwhile, organic solvents known in the art may be used, but the present disclosure is not limited thereto.

The lithium salt is dissolved in the organic solvent and may act as a source of the lithium ion in the battery to allow basic operation of a lithium secondary battery and to promote movement of lithium ions between a positive electrode and a negative electrode. A non-limiting example of the lithium salt may be LiPF₆, LiBF₄, LiSbF₆, LiAsF₆, LiN(SO₃C₂F₅)₂, LiN(CF₃SO₂)₂, LiC₄F₉SO₃, LiClO₄, LiAlO₂, LiAlCl₄, LiN(C_(x)F_(2x+1)SO₂) (C_(y)F_(2y+1)SO₂) (x and y are natural numbers), LiCl, LiI, LiB(C₂O₄)₂, or a combination thereof, but is not limited thereto. The concentration of the lithium salt may be in a range of 0.1 M to 5.0 M, or 0.1 M to 2.0 M. When the concentration of the lithium salt satisfies the range, the electrolyte solution has appropriate conductivity and viscosity, thereby showing excellent electrolyte solution performance and effectively improving lithium ion mobility.

In addition, the electrolyte solution may further include pyridine, triethylphosphate, triethanolamine, cyclic ether, ethylene diamine, n-glyme, hexaphosphate triamide, a nitrobenzene derivative, sulfur, a quinone imine dye, N-substituted oxazolidinone, N,N-substituted imidazolidine, ethylene glycol dialkyl ether, an ammonium salt, pyrrole, 2-methoxyethanol and aluminum trichloride, and the like, if necessary, for improving charge/discharge characteristics, flame retardant characteristics, and the like. In some cases, a halogen-containing solvent such as carbon tetrachloride and ethylene trifluoride may be further included for imparting non-flammability, and fluoro-ethylene carbonate (FEC), propene sultone (PRS), fluoro-propylene carbonate and FPC), and the like may be further included for improving conservation properties at a high temperature.

The separator is a separator having micropores formed to allow ions to pass through, and a non-limiting example thereof may be one or a combination of two or more selected from the group consisting of glass fiber, polyester, polyethylene, polypropylene, polytetrafluoroethylene, and the like and may be in a non-woven fabric or woven fabric form. Specifically, a polyolefin-based polymer separator such as polyethylene and polypropylene is mainly used in the lithium secondary battery, but is not limited thereto. In addition, a separator coated with a composition including a ceramic component or a polymer material may be used for securing thermal resistance or mechanical strength, the separator may be used optionally in a monolayer or multi-layer structure, and a separator known in the art may be used, but is not limited thereto.

The secondary battery according to an exemplary embodiment may have an expansion rate of 75% or less. Specifically, the expansion rate may be 65% or less, more specifically 55% or less, or 50% or less, and the lower limit is not particularly limited, but may be 0.1% or more. The secondary battery according to an exemplary embodiment satisfying the expansion rate range effectively prevents the separation and desorption of an active material and improves the structural stability of an electrode to suppress an increase in resistance by volume expansion even with a change in electrode volume occurring as charging and discharging progress, based on improved adhesive strength, and thus, may implement significantly improved charge/discharge cycle characteristics of a battery and battery performance.

The capacity retention rate after 50 cycles of charging and discharging of the secondary battery according to an exemplary embodiment may be 80% or more. Specifically, the capacity retention rate may be 85% or more or 90% or more. The secondary battery according to an exemplary embodiment satisfying the range may maintain a high capacity retention rate after charging and discharging, and suppress the expansion of the negative electrode, and effectively improve the charge/discharge cycle characteristics and performance of a secondary battery.

Hereinafter, the method of preparing a binder for a secondary battery according to the present invention will be described in detail.

The present disclosure provides a method of preparing a binder for a secondary battery including: (A) saponifying a copolymer including a repeating unit (a) of the following Chemical Formula 1 and a repeating unit (c) of the following Chemical Formula 3 to prepare a saponified copolymer; and

(B) reacting the saponified copolymer and a silane-based crosslinking agent to perform crosslinking,

wherein the saponified copolymer includes the repeating unit (a) of the following Chemical Formula 1, a repeating unit (b) of the following Chemical Formula 2, the repeating unit (c) of the following Chemical Formula 3, and a repeating unit (d) of the following Chemical Formula 4:

The detailed description of Chemical Formulae 1 to 4 is as described above, and thus, will be omitted.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the copolymer of step (A) may be prepared by copolymerizing vinyl acetate and alkyl (meth)acrylate, and may be prepared by various known methods such as emulsion polymerization, suspension polymerization, solution polymerization, or bulk polymerization. Otherwise, as the copolymer of step (A), commercially available products may be used without limitation.

The alkyl (meth)acrylate may be one or two or more selected from the group consisting of methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, n-butyl acrylate, isobutyl acrylate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, and the like. Otherwise, as the copolymer, commercially available products may be purchased and used.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the copolymer of step (A) may be a random copolymer in which the repeating unit (a) and the repeating unit (c) form a backbone, a block copolymer in which a repeating unit block is connected in a linear shape, or a tapered copolymer. Specifically, when the copolymer is a random copolymer, it has excellent solubility in water to improve processability when a negative electrode slurry composition for a secondary battery is manufactured, and has sufficient tensile strength and flexibility to improve the strength and the flexibility of the negative electrode active material layer, which is thus preferred.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the copolymer of step (A) may include a and c at a mole ratio fraction of a:c of 0.05 to 0.95:0.95 to 0.05, specifically 0.30 to 0.95:0.70 to 0.05, and more specifically 0.5 to 0.95:0.5 to 0.05, but is not limited thereto, wherein a and c are mole fractions of the repeating unit (a) and the repeating unit (c), respectively, in the copolymer.

In addition, the copolymer of step (A) may have a weight average molecular weight of 100,000 to 2,000,000 Da, specifically 200,000 to 1,800,000 Da. Otherwise, the copolymer of step (A) may have a weight average molecular weight of 400,000 to 1,600,000 Da. More specifically, the copolymer may have a weight average molecular weight of 500,000 to 1,500,000 Da, but is not limited thereto. The copolymer satisfying the range may have further improved adhesion of the binder for a secondary battery.

In addition, the copolymer of step (A) may include known repeating units other than the repeating unit (a) and the repeating unit (c), but is not limited thereto.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the saponification reaction may be used without limitation as long as it is known or commonly used, and specifically, may be performed by dissolving or dispersing the copolymer of step (A) in water with alcohol or hydrous alcohol and using an alkali catalyst or an acid catalyst, and the alcohol may be methanol, ethanol, propanol, tert-butanol, and the like without limitation, but specifically, may be methanol. The concentration of the copolymer in alcohol may be appropriately adjusted depending on the viscosity, but may satisfy in a range of 10 to 60 wt %. As the catalyst, alkali catalysts such as alkali metal hydroxides or alkylates such as sodium hydroxide, potassium hydroxide, sodium methylate, sodium ethylate, potassium methylate, and lithium methylate, and acid catalyst such as sulfuric acid, hydrochloric acid, nitric acid, methanesulfonic acid, zeolite, and cation exchange resin may be used. In addition, the reaction temperature of the saponification reaction is not particularly limited, but 10 to 80° C., specifically 20 to 70° C.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the degree of saponification in step (A) may be calculated by (b+d)/(a+b+c+d), and the calculated value may satisfy Equation 1, and specifically, may satisfy Equation 2, wherein a, b, c, and d are mole fractions of the repeating units (a), (b), (c), and (d) in the saponified copolymer. When the saponified copolymer satisfies Equation 1, specifically Equation 2, coatability, adhesive properties, and tensile strength may be further improved, and when the negative electrode slurry composition for a secondary battery is prepared by including the copolymer, the exfoliation and desorption of the negative electrode active material from a current collector may be effectively suppressed. In addition, the saponified copolymer satisfying the range is used to prepare a negative electrode slurry composition for a secondary battery and a negative electrode for a secondary battery, a binding force between the negative electrode active material and the current collector is effectively improved to effectively suppress the expansion of a negative electrode, thereby improving the charge/discharge cycle characteristics and the performance of a secondary battery, but the numerical value range of the degree of saponification is not limited thereto as long as the purpose of the present disclosure is achieved.

In addition, the saponified copolymer may include known repeating units other than the repeating unit (a) to the repeating unit (d), but is not limited thereto.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, a crosslinked binder which is a crosslinked product, that is, the binder for a secondary battery according to an exemplary embodiment may be prepared by step (B), and the crosslinked binder may be present in an aqueous state with an uncrosslinked copolymer(the saponified copolymer), but is not limited thereto.

In the method of preparing a binder for a secondary battery according to another exemplary embodiment, in step (B), a silane-based crosslinking agent is added to an aqueous solution including the saponified copolymer to perform a crosslinking reaction partly, and a remaining crosslinking reaction is performed by a subsequent step such as a drying step, thereby preparing a binder for a secondary battery.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the detailed description of the saponified copolymer and an example of the compound may be the same as or different from the description for the copolymer of the binder for a secondary battery above. In addition, since the detailed description of the silane-based crosslinking agent and an example and the content of the compound are as described above, they will be omitted.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the method of adding the silane-based crosslinking agent is not largely limited as long as it is a commonly used method or a known method, but, for example, a binder composition including a crosslinked binder may be prepared by dissolving the saponified copolymer in water to prepare an aqueous solution having a concentration of 5 to 50 wt %, adding the silane-based crosslinking agent dropwise for 10 minutes to 1 hour, and stirring the solution for 4 hours or more, but the present disclosure is not limited thereto.

In the method of preparing a binder for a secondary battery according to an exemplary embodiment, the saponified copolymer and the silane-based crosslinking agent may be added so that they satisfy the weight ratio of 80 to 99.9:20 to 0.1. Specifically, the silane-based crosslinking agent may be added so as to satisfy the weight ratio of 83 to 99:17 to 1, more specifically 85 to 95:15 to 5. When the content range is satisfied, the three-dimensional structure of the binder for a secondary battery may be formed to be more robust, and thus, the expansion of a negative electrode is suppressed to show a lower expansion rate and an improved capacity retention rate, thereby effectively improving the charge/discharge cycle characteristics and the performance of the secondary battery.

Hereinafter, the present invention will be described in more detail with reference to the examples and the comparative examples. However, the following examples and comparative examples are only one example for describing the present invention in more detail, and do not limit the present invention in any way.

The physical properties of the following examples and comparative examples of the present invention were measured by the following methods.

Method of Evaluating Physical Properties 1. Weight Average Molecular Weight [kDa]

The weight average molecular weight of the copolymers prepared in the examples and the comparative examples were measured using GPC (Agilent). Agilent Mixed C (×2ea) was used as a GPC column, tetrahydrofuran was used as a solvent, and polystyrene was used as a standard, and analysis was performed at room temperature, at a flow rate of 1 mL/min.

2. Tensile Strength [kgf/cm²] and Yield Strain [%]

The tensile strength and the yield strain of the binder compositions prepared in the examples and the comparative examples were measured in accordance with ASTM D638. A specimen obtained by cutting a film having a thickness of 50 μm into type IV was prepared, the measurement was performed under the conditions of a speed of 3 mm/min., and the measured values are listed in Table 1.

3. Adhesion Test [N/20 mm]

The adhesion of the negative electrodes manufactured in the examples and the comparative examples were measured using UTM. A rolled negative electrode surface was adhered to a tape, the measurement was performed under the conditions of an angle of 180° and a speed of 30 mm/min., and the measured values are listed in Table 1.

4. Negative Electrode Slurry Composition Coatability

The negative electrode slurry composition for a secondary battery prepared in the examples and the comparative examples were coated on a copper foil, and the coatability was evaluated based on the following criteria. The evaluation results are shown in the following Table 1.

⊚: coated in a uniform form throughout and no agglomerate observed

◯: coated in a uniform form throughout

(less than 5 agglomerates observed per unit area (100 mm×100 mm))

Δ: some agglomerates observed

(5 or more and less than 20 agglomerates observed per unit area (100 mmx100 mm))

x: many agglomerates observed

(20 or more agglomerates observed per unit area (100 mm×100 mm))

5. Evaluation of Battery Performance

A CR2016 coin type half cell was manufactured in the examples and the comparative examples and the electrochemical properties were evaluated.

1) Charge capacity [mAh/g] and discharge capacity [mAh/g] at cycle 1, and initial (charge and discharge) efficiency [%]

Secondary batteries manufactured in the examples and the comparative examples were charged and discharged once at 0.1 C between 0.01 V and 1.5 V to measure a charge capacity at cycle 1 (initial charge capacity)(mAh/g), a discharge capacity at cycle 1 (mAh/g), and initial (charge and discharge) efficiency (%) were measured, respectively, and the results are shown in the following Table 2.

2) Expansion rate (%)

The thickness (t₁) of the secondary battery negative electrodes manufactured in the examples and the comparative examples was measured, a secondary battery was manufactured and charged to 0.01 V at 0.1 C-rate, and a half cell was disassembled to measure the thickness (t2) of the negative electrode after charging. The expansion rate of the negative electrode was calculated by the following calculation formula, and the calculated expansion rate is shown in the following Table 2.

Expansion rate (%)=(t₂−t₁)/(t₁−current collector thickness)×100   [Calculation Formula]

wherein a current collector thickness is the thickness of a negative electrode current collector used in the manufacture of the secondary battery negative electrode.

3) Capacity retention rate [%] after charging and discharging of 50 cycles

The secondary batteries manufactured in the examples and the comparative examples were charged and discharged three times at 0.1 C between 0.01 V and 1.5 V, and 50 cycles of charging and discharging to 0.5 C between 0.01 V and 1.0 V were performed to evaluate the charge/discharge cycle characteristics of the batteries. During the charging, CV current conditions were 0.01 C CV cutoff. The charge/discharge cycle characteristics were obtained by measuring a capacity retention rate after 50 cycles of charging and discharging, specifically by showing a ratio (%) of a discharge capacity after repeating 50 cycles of charging and discharging to an initial discharge capacity. The results are shown in the following Table 2.

EXAMPLE 1 Preparation of Copolymer and Binder Composition

90 g of water, 0.91 g of sodium dodecylbenzenesulfonate, and 0.13 g of sodium hydrogen carbonate were added to a round bottom flask under a nitrogen atmosphere and stirring was performed. The temperature was raised to 65° C. with stirring, 0.05 g of potassium persulfate was added thereto, 33.5 g of vinyl acetate and 16.5 g of methyl acrylate were added thereto for 3 hours, stirring was further performed for 2 hours, and the polymerization was completed. 450 g of a saturated sodium chloride aqueous solution was added to the polymerization solution to agglomerate a copolymer, and filtration and drying were performed to obtain 42 g of vinyl acetate/methyl acrylate copolymer. The obtained polymer was dissolved in tetrahydrofuran, filtration was performed with a filter, and a weight average molecular weight was determined to be 740 kDa by a molecular weight measurement device (GPC, RI detector).

30 g of the copolymer, 150 ml of methanol, and 12.5 g of sodium hydroxide were added to 150 ml of water and completely dissolved therein, and stirring was performed at 60° C. for 12 hours to perform a saponification reaction. Next, the saponified copolymer was subjected to solidification in 1 L of ethanol, filtration, and drying steps, thereby finally obtaining a saponified copolymer having a mole composition ratio of vinyl acetate/vinyl alcohol/methyl acrylate/sodium acrylic acid of 18/49/7/26. The composition ratio was confirmed by ¹³C-NMR.

9 g of the saponified copolymer was added to 90 g of water, and stirring was performed at 60° C. for 6 hours to dissolve the copolymer, thereby preparing an aqueous solution. Next, 1 g of diethoxydimethylsilane was added dropwise to an aqueous solution in which the saponified copolymer was dissolved for 1 hour, and the solution was further stirred for 4 hours to obtain a binder composition including a crosslinked binder (crosslinked product). The tensile strength of the prepared binder composition was measured, and is listed in the following Table 1.

Manufacture of Secondary Battery Negative Electrode

A negative electrode active material, a CNT-based conductive material, and the binder composition prepared above (solid content: 10%) were added to water at a weight ratio satisfying 95.75:0.25:4.0, and were mixed, thereby preparing a negative electrode slurry composition for a secondary battery (solid content: 50%). At this time, they were added so that the weight ratio was satisfied based on the solid content (dry weight) of the binder composition. Specifically, a mixture of 15 wt % of a silicon-based active material (SiC) having an average particle diameter of 6 μm and 85 wt % of graphite (artificial graphite having an average particle diameter (D50) of 13 μm) was used as the negative electrode active material, a SW-CNT-based conductive material having an average length of 5 μm was used as the CNT-based conductive material, and a negative electrode slurry composition satisfying the weight ratio was dispersed by performing sufficient stirring at a speed of 45 rpm for 30 minutes or more using a planetary mixer. The thus-prepared negative electrode slurry composition was applied to a negative electrode current collector (thickness: 10 μm) at an application amount of 5.6 mg/cm², dried in a vacuum oven at 70° C. for 10 hours, and rolled under the conditions of a temperature of 50° C. and a pressure of 15 MPa, thereby manufacturing a negative electrode having a final thickness of 50 μm. The adhesion of the negative electrode was measured and is listed in the following Table 1.

Manufacture of Coin Cell (Secondary Battery)

A polyethylene separator (thickness: 20 μm) was interposed between the negative electrode manufactured above and a lithium metal (thickness: 1 mm), and 1 M LiPF₆ dissolved in a mixed solvent including ethylene carbonate (EC)/fluoroethylene carbonate (FEC)/ethylmethyl carbonate (EMC)/diethyl carbonate (DEC) at a volume ratio of 20/10/20/50 was used as an electrolyte solution, thereby manufacturing a coin cell-type half battery (CR2016 coin half cell) according to a common manufacturing method. Battery performance was evaluated and is listed in the following Table 2.

EXAMPLE 2

The process was performed in the same manner as in Example 1, except that 3-glycidoxypropyldimethoxymethylsilane was used instead of diethoxydimethylsilane as the silane-based crosslinking agent. The measured physical properties are shown in the following Tables 1 and 2.

EXAMPLE 3

The process was performed in the same manner as in Example 1, except that (3-glycidyloxypropyl)trimethoxysilane was used instead of diethoxydimethylsilane as the silane-based crosslinking agent. The measured physical properties are shown in the following Tables 1 and 2.

EXAMPLE 4

The process was performed in the same manner as in Example 1, except that (3-aminopropyl)triethoxysilane was used instead of diethoxydimethylsilane as the silane-based crosslinking agent. The measured physical properties are shown in the following Tables 1 and 2.

EXAMPLE 5

The process was performed in the same manner as in Example 1, except that [3-(2-aminoethylamino)propyl]trimethoxysilane was used instead of diethoxydimethylsilane as the silane-based crosslinking agent. The measured physical properties are shown in the following Tables 1 and 2.

EXAMPLE 6

The process was performed in the same manner as in Example 1, except that 3-(triethoxysilyl)propionitrile was used instead of diethoxydimethylsilane as the silane-based crosslinking agent. The measured physical properties are shown in the following Tables 1 and 2.

EXAMPLE 7

The process was performed in the same manner as in Example 1, except that 9.8 g of sodium hydroxide was used during the saponification reaction. The mole composition ratio of the synthesized copolymer of vinyl acetate/vinyl alcohol/methyl acrylate/sodium acrylic acid was 29/38/10/23. The measured physical properties are shown in the following Tables 1 and 2.

EXAMPLE 8

The process was performed in the same manner as in Example 1, except that 6.5 g of sodium hydroxide was used during the saponification reaction. The mole composition ratio of the synthesized copolymer of vinyl acetate/vinyl alcohol/methyl acrylate/sodium acrylic acid was 41/26/19/14. The measured physical properties are shown in the following Tables 1 and 2.

EXAMPLE 9

The process was performed in the same manner as in Example 1, except that 40 g of vinyl acetate and 10 g of methyl acrylate were used. The weight average molecular weight of the synthesized copolymer of vinyl acetate/methyl acrylate was 650 kDa, and the mole composition ratio of the copolymer of vinyl acetate/vinyl alcohol/methyl acrylate/sodium acrylic acid was 19/61/7/18. The measured physical properties are shown in the following Tables 1 and 2.

EXAMPLE 10

The process was performed in the same manner as in Example 1, except that 16.5 g of vinyl acetate and 33.5 g of methyl acrylate were used. The weight average molecular weight of the synthesized copolymer of vinyl acetate/methyl acrylate was 830 kDa, and the mole composition ratio of the copolymer of vinyl acetate/vinyl alcohol/methyl acrylate/sodium acrylic acid was 8/25/10/57. The measured physical properties are shown in the following Tables 1 and 2.

COMPARATIVE EXAMPLE 1

The process was performed in the same manner as in Example 1, except that polyvinyl alcohol (PVA) (Sigma Aldrich) was used instead of the saponified copolymer. The measured physical properties are shown in the following Tables 1 and 2.

COMPARATIVE EXAMPLE 2

The process was performed in the same manner as in Example 1, except that polyacrylic acid sodium salt (PAANa) (Sigma Aldrich) was used instead of the saponified copolymer. The measured physical properties are shown in the following Tables 1 and 2.

COMPARATIVE EXAMPLE 3

The process was performed in the same manner as in Example 1, except that a mixture of styrene-butadiene rubber (SBR) (Sigma Aldrich) and carboxymethyl cellulose sodium salt (CMC) (Sigma Aldrich) combined at a weight ratio of 1:1 was used instead of the binder composition in the manufacture of a secondary battery negative electrode. The measured physical properties are shown in the following Tables 1 and 2.

COMPARATIVE EXAMPLE 4

A binder composition was prepared in the same manner as in Example 1, except that when the copolymer was synthesized, polymerization was performed by adding 2 g of a styrene monomer into the monomer mixture of vinyl acetate and methyl acrylate, and then 10 g of the thus-prepared copolymer was added to 90 g of water, and stirring was performed at 60° C. for 6 hours to perform. The tensile strength of the prepared binder composition was measured, and is listed in the following Table 1.

In addition, a negative electrode for a secondary battery was manufactured in the same manner as in Example 1, except that the binder prepared above was used instead of the crosslinked binder. The measured physical properties are shown in the following Tables 1 and 2.

COMPARATIVE EXAMPLE 5

The process was performed in the same manner as in Example 1, except that no silane-based crosslinking agent was added. The measured physical properties are shown in the following Tables 1 and 2.

TABLE 1 Degree of Weight average saponification molecular Tensile Yield Slurry (b + d)/(a + weight (Mw, strength strain Adhesion composition b + c + d) kDa) (kgf/cm²) (%) (N/20 mm) coatability Example 1 0.75 740 932 4.5 4.33 ◯ Example 2 0.75 740 1087 4.6 4.46 ◯ Example 3 0.75 740 1114 5.1 4.58 ◯ Example 4 0.75 740 1267 5.2 4.96 ⊚ Example 5 0.75 740 1186 5.0 4.82 ⊚ Example 6 0.75 740 1371 4.3 4.51 ◯ Example 7 0.61 740 898 5.5 4.64 ◯ Example 8 0.40 770 798 5.1 3.74 ◯ Example 9 0.74 650 949 5.2 4.90 ⊚ Example 10 0.82 830 1410 4.3 4.68 ◯ Comparative 1 205 760 6.1 2.44 X Example 1 Comparative 1  83 1600 1.3 2.14 X Example 2 Comparative — — 115 192 2.51 Δ Example 3 Comparative 0.76 450 989 3.3 2.41 ◯ Example 4 Comparative 0.75 740 1340 4.0 4.01 ◯ Example 5

In Tables 1, it was confirmed that the examples had excellent tensile strength and adhesion of the binder for a secondary battery, and when a negative electrode slurry composition including the binder was prepared, the composition had no agglomeration and excellent coatability.

TABLE 2 Capacity retention rate (%) after 50 1 cycle 1 cycle cycles of charge discharge Initial Expansion charging capacity capacity efficiency rate and dis- (mAh/g) (mAh/g) (%) (%) charging Example 1 632 583 92.2 54 82 Example 2 629 581 92.4 51 84 Example 3 629 583 92.7 46 88 Example 4 627 581 92.7 37 95 Example 5 627 580 92.5 43 92 Example 6 626 579 92.5 42 87 Example 7 628 580 92.4 56 82 Example 8 628 579 92.2 64 79 Example 9 631 580 92.1 41 93 Example 10 626 580 92.7 42 83 Comparative 621 564 90.8 85 68 Example 1 Comparative 614 555 90.4 87 61 Example 2 Comparative 631 584 92.6 78 64 Example 3 Comparative 626 577 92.2 70 71 Example 4 Comparative 627 579 92.3 61 78 Example 5

In Table 2, it was confirmed that the binder for a secondary battery according to an exemplary embodiment improved a binding force between a negative electrode current collector and a negative electrode active material by the excellent coatability and adhesion, and had a significantly low expansion rate and an effectively improved capacity retention rate after 50 cycles of charging and discharging, as compared with the comparative examples.

In particular, in Example 4 using the silane-based crosslinking agent, expansion rate and capacity retention rate after 50 cycles were effectively improved, as compared with Comparative Example 5 which did not use the silane-based crosslinking agent, and it was confirmed therefrom that since the silane-based crosslinking agent was added, the binder for a secondary battery described above formed a three-dimensional crosslinked structure, thereby exerting the physical properties to be desired in the present invention.

Thus, the binder for a secondary battery according to the present invention improves a binding force between the negative electrode current collector and the negative electrode active material to obtain an effect of suppressing the exfoliation and desorption of the negative electrode active material, effectively suppress the expansion of the negative electrode to improve the charge/discharge cycle characteristics and the performance of a secondary battery.

An object of the present disclosure may provide a binder for a secondary battery having improved mechanical properties and adhesion properties of a binder for a secondary battery, a negative electrode slurry composition for a secondary battery including the same, a negative electrode manufactured using the same, and a secondary battery including the negative electrode.

Accordingly, the binder for a secondary battery according to an exemplary embodiment provides a novel binder having a three-dimensional structure using a silane-based crosslinking agent, and when it is applied to a negative electrode and a secondary battery, the expansion of the negative electrode is suppressed, and the charge/discharge cycle characteristics and the performance of the secondary battery are significantly improved.

The binder for a secondary battery according to an exemplary embodiment, the negative electrode including the same, and the secondary battery including the negative electrode have excellent thermal resistance and mechanical properties, an improved binding force, and excellent electrical properties.

In addition, the binder for a secondary battery according to an exemplary embodiment has improved coatability and adhesion to suppress the exfoliation and desorption of the negative electrode active material, thereby improving the performance of the secondary battery.

Hereinabove, although the present invention has been described by specified matters and specific exemplary embodiments, they have been provided only for assisting in the entire understanding of the present invention. Therefore, the present invention is not by the specific matters limited to the exemplary embodiments. Various modifications and changes may be made by those skilled in the art to which the present invention pertains from this description.

Therefore, the spirit of the present invention should not be limited to the above-described exemplary embodiments, and the following claims as well as all modified equally or equivalently to the claims are intended to fall within the scope and spirit of the invention. 

What is claimed is:
 1. A binder for a secondary battery, the binder comprising a copolymer which is crosslinked with a silane-based crosslinking agent, wherein the copolymer comprises a repeating unit (a) of the following Chemical Formula 1, a repeating unit (b) of the following Chemical Formula 2, a repeating unit (c) of the following Chemical Formula 3, and a repeating unit (d) of the following Chemical Formula 4:

wherein R₁ and R₃ are independently substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms; R₂ and R₄ are independently hydrogen or substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms; M^(n+) is a cation having an oxidation number of n except for a hydrogen ion; and n is an integer of 1 to
 3. 2. The binder for a secondary battery of claim 1, wherein (a+b):(c+d) of the copolymer is 0.05 to 0.95:0.95 to 0.05, in which a, b, c, and d are mole fractions of the repeating units (a), (b), (c), and (d), respectively in the copolymer.
 3. The binder for a secondary battery of claim 1, wherein the copolymer satisfies the following Equation 1: 0.45 21 (b+d)/(a+b+c+d)<1.0   [Equation 1] wherein a, b, c, and d are mole fractions of the repeating units (a), (b), (c), and (d), respectively in the copolymer.
 4. The binder for a secondary battery of claim 1, wherein the silane-based crosslinking agent is represented by the following Chemical Formula 5: (R₅O)_(x)Si(R₆)_(y)   [Chemical Formula 5] wherein x+y=4, and x is 2 or 3; R₅ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms; R₆ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms or heterohydrocarbyl having 1 to 7 carbon atoms; the hydrocarbyl and the heterohydrocarbyl may be optionally substituted by one or more selected from glycidyl, amino, and cyano; and when y is 2, each R₆ may be the same as or different from each other.
 5. The binder for a secondary battery of claim 1, wherein the silane-based crosslinking agent is one or a combination of two or more selected from the group consisting of dimethyldimethoxysilane, diethoxydimethylsilane, methyltriethoxysilane, (3-glycidoxypropyl)methyldimethoxysilane, (3-glycidoxypropyl)methyldiethoxysilane, (3-glycidoxypropyl)trimethoxysilane, (3-glycidoxypropyl)triethoxysilane, (3-aminopropyl)methyldimethoxysilane, (3-aminopropyl)methyldiethoxysilane, (3-aminopropyl)trimethoxysilane, (3-aminopropyl)triethoxysilane, [3-(2-aminoethylamino)propyl]methyldimethoxysilane, [3-(2-aminoethylamino)propyl]methyldiethoxysilane, [3-(2-aminoethylamino)propyl]triethoxysilane, [3-(2-aminoethylamino)propyl]trimethoxysilane, 3-(trimethoxysilyl)propionitrile, and 3-(triethoxysilyl)propionitrile.
 6. The binder for a secondary battery of claim 1, wherein the silane-based crosslinking agent is one or a combination of two selected from the group consisting of (3-aminopropyl)triethoxysilane and [3-(2-aminoethylamino)propyl]trimethoxysilane.
 7. The binder for a secondary battery of claim 1, wherein the silane-based crosslinking agent is comprised at 0.1 to 20 wt % with respect to the binder for a secondary battery.
 8. The binder for a secondary battery of claim 1, wherein the binder for a secondary battery is a binder for a lithium secondary battery negative electrode.
 9. A secondary battery comprising: a positive electrode and a negative electrode for a secondary battery, wherein the negative electrode for a secondary battery comprises a current collector; and a negative electrode active material layer disposed on the current collector, and the negative electrode active material layer comprises the binder for a secondary battery of claim 1 and a negative electrode active material.
 10. The secondary battery of claim 9, wherein the negative electrode active material comprises a silicon-based active material.
 11. The secondary battery of claim 10, wherein the negative electrode active material further comprises a graphite-based active material.
 12. The secondary battery of claim 11, wherein a mass ratio between the silicon-based active material and the graphite-based active material is 97:3 to 3:97.
 13. The secondary battery of claim 9, wherein the binder for a secondary battery is comprised at 0.1 to 30 wt % with respect to the negative electrode active material layer.
 14. A method of preparing a binder for a secondary battery, the method comprising the steps of: step (A) saponifying a copolymer comprising a repeating unit (a) of the following Chemical Formula 1 and a repeating unit (c) of the following Chemical Formula 3 to prepare a saponified copolymer; and step (B) reacting the saponified copolymer and a silane-based crosslinking agent to perform crosslinking, wherein the saponified copolymer comprises the repeating unit (a) of the following Chemical Formula 1, a repeating unit (b) of the following Chemical Formula 2, the repeating unit (c) of the following Chemical Formula 3, and a repeating unit (d) of the following Chemical Formula 4:

wherein R₁ and R₃ are independently substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms; R₂ and R₄ are independently hydrogen or substituted or unsubstituted hydrocarbyl having 1 to 10 carbon atoms; M^(n+) is a cation having an oxidation number of n except for a hydrogen ion; and n is an integer of 1 to
 3. 15. The method of preparing a binder for a secondary battery of claim 14, wherein a degree of saponification in step (A) is more than 0.45 and less than 1.0, and the degree of saponification is calculated by (b+d)/(a+b+c+d), in which a, b, c, and d are mole fractions of the repeating units (a), (b), (c), and (d) in the saponified copolymer.
 16. The method of preparing a binder for a secondary battery of claim 14, wherein the silane-based crosslinking agent is represented by the following Chemical Formula 5: (R₅O)_(x)Si(R₆)_(y)   [Chemical Formula 5] wherein x+y=4, and x is 2 or 3; R₅ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms; R₆ is substituted or unsubstituted hydrocarbyl having 1 to 7 carbon atoms or heterohydrocarbyl having 1 to 7 carbon atoms; the hydrocarbyl and the heterohydrocarbyl may be optionally substituted by one or more selected from glycidyl, amino, and cyano; and when y is 2, each R₆ may be the same as or different from each other.
 17. The method of preparing a binder for a secondary battery of claim 14, wherein the silane-based crosslinking agent is one or a combination of two or more selected from the group consisting of dimethyldimethoxysilane, diethoxydimethylsilane, methyltriethoxysilane, (3-glycidoxypropyl)methyldimethoxysilane, (3-glycidoxypropyl)methyldiethoxysilane, (3-glycidoxypropyl)trimethoxysilane, (3-glycidoxypropyl)triethoxysilane, (3-aminopropyl)methyldimethoxysilane, (3-aminopropyl)methyldiethoxysilane, (3-aminopropyl)trimethoxysilane, (3-aminopropyl)triethoxysilane, [3-(2-aminoethylamino)propyl]methyldimethoxysilane, [3-(2-aminoethylamino)propyl]methyldiethoxysilane, [3-(2-aminoethylamino)propyl]triethoxysilane, [3-(2-aminoethylamino)propyl]trimethoxysilane, 3-(trimethoxysilyl)propionitrile, and 3-(triethoxysilyl)propionitrile.
 18. The method of preparing a binder for a secondary battery of claim 14, wherein the silane-based crosslinking agent is one or a combination of two selected from the group consisting of (3-aminopropyl)triethoxysilane and [3-(2-aminoethylamino)propyl]trimethoxysilane.
 19. The method of preparing a binder for a secondary battery of claim 14, wherein the silane-based crosslinking agent is comprised at 0.1 to 20 wt % with respect to the binder for a secondary battery. 